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August 1, 2004Prenatal Diagnosis

A case of ring chromosome 22 with deletion of the 22q13.3 region associated with agenesis of the corpus callosum, fornix and septum pellucidum

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Authors

JDJosé DelcánUniversidad Rey Juan CarlosMOMaría OreraUniversidad Complutense de MadridRLRafael LinaresUniversidad Rey Juan Carlos

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Delcán et al. (2004) studied this question.

synapsesocial.com/papers/6a89b6ab176d2ac34cfbb269https://doi.org/10.1002/pd.955
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Two 22q telomere deletions serendipitously detected by FISH.1998 · 83 citations
  2. 2Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype2000 · 104 citations
  3. 3Characterization of a human gene related to genes encoding somatostatin receptors1996 · 105 citations
  4. 4Multiple congenital anomaly/mental retardation (MCA/MR) syndrome with Goldenhar complex due to a terminal del(22q)1988 · 78 citations
  5. 5AGENESIS OF ThE CORPUS CALLOSUM ASSOCIATED WITH RELAPSING HYPOTHERMIA A CLINICO-PATHOLOGICAL REPORT1973 · 42 citations